Reacción #487536

ord-68d3820112a24757b483548930ce0911

Ecuación de reacción

Cc1ccc(S(=O)(=O)Cl)cc1
TsCl
CCN(CC)CC
triethylamine
Cc1ccc(S(=O)(=O)Cl)cc1
TsCl
CCOP(=O)(OCC)C(F)(F)CCO
Diethyl 3-hydroxy-1,1-difluoro-propylphosphonate
CCOP(=O)(OCC)C(F)(F)CCOS(=O)(=O)c1ccc(C)cc1
Diethyl 3-tosyloxy-1,1-difluoro-propylphosphonate

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroAfter 30 m, the reaction mixture was partitioned between water and CH2Cl2
  2. 2
    FiltraciónThe organic layer was filtered
  3. 3
    Concentraciónconcentrated in vacuo
  4. 4
    workup.DISSOLUTIONThe residue was dissolved in 1:1 hexanes
  5. 5
    LavadoThe column was eluted with hexanes-ethyl acetate

Procedimiento

Diethyl 3-hydroxy-1,1-difluoro-propylphosphonate [1225194-19-3](4.4 g, 0.019 mol) was dissolved in CH2Cl2 (20 mL) and triethylamine (7.7 g) and treated with TsCl (5.4 g, 0.029 mol) followed by DMAP (0.23 g, 0.0019 mol) at rt for 2 h. After 2 h, an additional portion of TsCl (0.6 g) was added. After 30 m, the reaction mixture was partitioned between water and CH2Cl2. The organic layer was filtered and concentrated in vacuo. The residue was dissolved in 1:1 hexanes:CH2Cl2 (100 mL) and applied to 85 g flash silica gel (topped with Na2SO4 and equilibrated with hexanes). The column was eluted with hexanes-ethyl acetate. Intermediate 23 weighed 6.3 g (94%). 1H NMR (CDCl3) 7.2-7.8 (AB, 4H); 3.9-4.4 (m, 6H); 2.0-3.0 (m, 5H), 1.4 (t, 6H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08741875B2uspto-grants-2014_06